Generic placeholder image

Medicinal Chemistry


ISSN (Print): 1573-4064
ISSN (Online): 1875-6638

Review Article

Therapeutic Monoclonal Antibodies and Multiple Sclerosis: The Essentials

Author(s): Ioannis Heliopoulos* and Athanasia Patousi

Volume 14 , Issue 2 , 2018

Page: [144 - 154] Pages: 11

DOI: 10.2174/1573406413666170906121828

Price: $65


Background: Monoclonal antibodies (mAbs) are now established as targeted therapies for malignancies, transplant rejection, autoimmune and infectious diseases. Two monoclonal antibodies are available for treatment and other antibodies are currently being tested in multiple sclerosis (MS) patients.

Objectives: The purpose of the present review paper is to outline the antibody engineering technologies, the immunologic and pharmacologic concepts of mbs and the current status of treatment in MS with emphasis on clinical efficacy and safety.

Method: We conducted a through review of the scientific literature published until 31 December 2014 (print and electronic publications) concerning the production, applications and side effects of the use of Mabs. Sixty five articles were used in total (both original research and review papers).

Conclusion: With the introduction of mAbs the treatment of MS has entered a new era, both with respect to efficacy and target specificity. However, administration of mAbs carries the risk of immune reactions such as acute anaphylaxis, serum sickness, infection and other autoimmune diseases. In addition, unexpected consequences arise from our incomplete knowledge of the immune system. For example, natalizumab, a monoclonal antibody targeting α4-integrin on leukocytes increases the risk of developing progressive multifocal leukoencephalopathy, without causing notable immunosuppression. Further study on the use of mabs is required, both in vitro and in the clinical field, in order to increase our knowledge upon these new revolutionary therapeutic agents.

Keywords: Alemtuzumab, daclizumab, monoclonal antibodies, natalizumab, ocrelizumab, ofatumumab, phage peptide libraries, rituximab, transgenic mice.

Graphical Abstract

Rights & Permissions Print Export Cite as
© 2022 Bentham Science Publishers | Privacy Policy